Product Details

SNP ID

rs74102304

Assay Type

Functionally tested

NCBI dbSNP Submissions

35

Location

Chr.1:99993576 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACAATGTTCGCCAACCTAAAATAC[A/G]TTTCCCTGGGAATTTTGGTCTTTCA

Phenotype

MIM: 605632

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC35A3 PubMed Links

Gene Details

Gene

SLC35A3

Gene Name

solute carrier family 35 member A3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271684.1	836	Missense Mutation	ATT,GTT	I8V	NP_001258613.1
NM_001271685.1	836	Missense Mutation	ATT,GTT	I50V	NP_001258614.1
NM_012243.2	836	Missense Mutation	ATT,GTT	I8V	NP_036375.1
XM_005270691.4	836	Missense Mutation	ATT,GTT	I8V	XP_005270748.1
XM_011541135.2	836	Missense Mutation	ATT,GTT	I50V	XP_011539437.1
XM_011541136.2	836	Missense Mutation	ATT,GTT	I8V	XP_011539438.1
XM_011541137.2	836	Missense Mutation	ATT,GTT	I50V	XP_011539439.1
XM_011541138.2	836	Missense Mutation	ATT,GTT	I50V	XP_011539440.1
XM_017000869.1	836	Missense Mutation	ATT,GTT	I8V	XP_016856358.1
XM_017000870.1	836	Missense Mutation	ATT,GTT	I8V	XP_016856359.1
XM_017000871.1	836	Missense Mutation	ATT,GTT	I8V	XP_016856360.1
XM_017000872.1	836	UTR 5			XP_016856361.1

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